Bulvalen (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Bulvalen" in Czech language version.

refsWebsite
Global rank Czech rank
2nd place
4th place
4th place
8th place
18th place
99th place
1,248th place
807th place
6,572nd place
low place
1st place
1st place

acs.org

pubs.acs.org

  • H. E. Zimmerman; R. W. Binkley; R. S. Givens; M. A. Sherwin. Mechanistic Organic Photochemistry. XXIV. The Mechanism of the Conversion of Barrelene to Semibullvalene. A General Photochemical Process. Journal of the American Chemical Society. 1967, s. 3932–3933. Dostupné online. doi:10.1021/ja00991a064. 

doi.org

  • Addison Ault. The Bullvalene Story. The Conception of Bullvalene, a Molecule That Has No Permanent Structure. Journal of Chemical Education. 2001, s. 924. doi:10.1021/ed078p924. Bibcode 2001JChEd..78..924A. 
  • J. Oth; K. Mullen; J. Gilles; G. Schröder. Comparison of 13C- and 1H- magnetic resonance spectroscopy as techniques for the quantitative investigation of dynamic processes. The Cope rearrangement in bullvalene. Helvetica Chimica Acta. 1974, s. 1415–1433. doi:10.1002/hlca.19740570518. 
  • W. Von Eggers Doering; Joel W. Rosenthal. 9,10-Dihydronaphthalene. Formation from Bullvalene and Nenitzescu's Hydrocarbon, Thermal Reorganization, and Photorearrangement to Bullvalene. Journal of the American Chemical Society. 1966, s. 2078–2079. doi:10.1021/ja00961a061. 
  • A. R. Lippert; J. Kaeobamrung; J. W. Bode. Synthesis of Oligosubstituted Bullvalones: Shapeshifting Molecules Under Basic Conditions. Journal of the American Chemical Society. 2006, s. 14738–14739. doi:10.1021/ja063900+. PMID 17105247. 
  • H. E. Zimmerman; G. L. Grunewald. The Chemistry of Barrelene. III. A Unique Photoisomerization to Semibullvalene. Journal of the American Chemical Society. 1966, s. 183–184. doi:10.1021/ja00953a045. 
  • H. E. Zimmerman; R. W. Binkley; R. S. Givens; M. A. Sherwin. Mechanistic Organic Photochemistry. XXIV. The Mechanism of the Conversion of Barrelene to Semibullvalene. A General Photochemical Process. Journal of the American Chemical Society. 1967, s. 3932–3933. Dostupné online. doi:10.1021/ja00991a064. 
  • C. Wang; J. Yuan; G. Li; Z. Wang; S. Zhang; Z. Xi. Metal-Mediated Efficient Synthesis, Structural Characterization, and Skeletal Rearrangement of Octasubstituted Semibullvalenes. Journal of the American Chemical Society. 2006, s. 4564–4565. doi:10.1021/ja0579208. PMID 16594680. 

harvard.edu

adsabs.harvard.edu

mcmaster.ca

fhs.mcmaster.ca

nih.gov

ncbi.nlm.nih.gov

  • A. R. Lippert; J. Kaeobamrung; J. W. Bode. Synthesis of Oligosubstituted Bullvalones: Shapeshifting Molecules Under Basic Conditions. Journal of the American Chemical Society. 2006, s. 14738–14739. doi:10.1021/ja063900+. PMID 17105247. 
  • C. Wang; J. Yuan; G. Li; Z. Wang; S. Zhang; Z. Xi. Metal-Mediated Efficient Synthesis, Structural Characterization, and Skeletal Rearrangement of Octasubstituted Semibullvalenes. Journal of the American Chemical Society. 2006, s. 4564–4565. doi:10.1021/ja0579208. PMID 16594680. 

web.archive.org